Jonsson J R, Klemm S A, Tunny T J, Stowasser M, Gordon R D
Hypertension Unit, Greenslopes Hospital, Brisbane, Australia.
Biochem Biophys Res Commun. 1995 Feb 15;207(2):565-71. doi: 10.1006/bbrc.1995.1225.
In Familial Hyperaldosteronism Type I (FH-I, glucocorticoid-suppressible hyperaldosteronism), a curable form of hypertension inherited in an autosomal dominant fashion, the underlying genetic defect is a "hybrid gene" in which 11 beta-hydroxylase gene regulatory elements are fused to the coding region of the aldosterone synthase gene. The detection of this hybrid gene by Southern blotting is time consuming and involves the use of radioactive isotopes. We describe a new, long polymerase chain reaction-based method for detecting the hybrid gene which greatly reduces the time required to obtain a result, avoids exposure of laboratory workers to radioactive materials, and will thereby facilitate the screening of patients for the presence of FH-I.
在I型家族性醛固酮增多症(FH-I,糖皮质激素可抑制性醛固酮增多症)中,这是一种以常染色体显性方式遗传的可治愈的高血压形式,潜在的基因缺陷是一种“杂交基因”,其中11β-羟化酶基因调控元件与醛固酮合酶基因的编码区域融合。通过Southern印迹法检测这种杂交基因既耗时又涉及放射性同位素的使用。我们描述了一种基于长聚合酶链反应的新方法来检测杂交基因,该方法大大减少了获得结果所需的时间,避免实验室工作人员接触放射性物质,从而有助于对患者进行FH-I的筛查。